The Recall Desk

State

Missouri product recalls

73,741 recalls have nationwide distribution and so reach Missouri. 8,500 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,500
Critical
1,339
Severe
2,203
Most recent
2026-10-28

Of the 8,500 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,203 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,500 recalls whose distribution notice names Missouri specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35651–35675 of 82241

  • ModerateFDA (Devices)·Z-2445-2019·2019-09-11

    Roche Tina-Quant Myoglobin Gen. 2 Assay Recalled for QC Imprecision

    Roche is recalling Tina-Quant Myoglobin Gen. 2 assays due to signal drops causing calibration failures and QC imprecision on specific analyzers.

    Product
    The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric assay for the quantitative in vitro determination of myoglobin in human serum and plasma on Roche automated clinical chemistry analyzers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2447-2019·2019-09-11

    Karl Storz Flexible Intubation Fiberscopes Recalled for Manufacturing Defect

    Karl Storz Endoscopy is recalling 14 Flexible Intubation Fiberscopes because they were improperly manufactured with a double port luer instead of a single port luer.

    Product
    Flexible Intubation Fiberscope, Model # 11301AB1
    Category
    Medical Device
    Distribution
    9 states
  • LowFDA (Devices)·Z-2475-2019·2019-09-11

    Alere Cholestech LDX Analyzer Recalled for Reversed Power Supply Polarity

    Alere San Diego, Inc. is recalling 186 Alere Cholestech LDX Analyzer kits because the power supplies have reversed polarity, rendering the devices inoperable.

    Product
    Alere Cholestech LDX Analyzer, model # 14-874 containing power supplies with the identifying codes of 1837d and 1843d - Product Usage: The Alere Cholestech LDX System is a small, portable analyzer and test cassette system. The System is for in vitro diagnostic use only. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2433-2019·2019-09-11

    Getinge CO2 Absorber Recalled for Reversed Expiration and Manufacturing Dates

    Getinge is recalling 1,444 boxes of disposable CO2 absorbers because the expiration and manufacturing dates on the labels are reversed.

    Product
    Getinge MCC Flow i Disposable CO2 absorber, used in anesthesia systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·091-2019·2019-09-10

    Hy-Vee Recalls Ready-to-Eat Beef and Chicken for Undeclared Milk

    Hy-Vee Fresh Commissary is recalling ready-to-eat beef and chicken products because they contain undeclared milk, a known allergen.

    Product
    HY-VEE FRESH COMMISSARY — Hy-Vee Fresh Commissary Recalls Ready-To-Eat Beef and Chicken Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    8 states
  • HighCPSC·19204·2019-09-10

    Ragdoll & Rockets Recalls Children's Loungewear for Flammability Violation

    Ragdoll & Rockets is recalling about 14,100 units of children's loungewear because the items fail to meet federal flammability standards for sleepwear, posing a risk of burn injuries.

    Product
    Children's loungewear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19200·2019-09-10

    Healing Solutions Recalls Essential Oils for Child-Resistant Packaging Failure

    Healing Solutions is recalling Wintergreen and Birch essential oils because the bottles lack required child-resistant caps, posing a poisoning risk to young children.

    Product
    Healing Solutions Wintergreen and Birch 100 percent Pure Therapeutic Grade Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19203·2019-09-10

    DIANA Stormrider Gen 2 Air Rifles Recalled for Unexpected Discharge Risk

    DIANA is recalling Stormrider Gen 2 air rifles because they can unexpectedly discharge even when the safety is engaged, posing a risk of serious injury or death.

    Product
    DIANA® Stormrider Gen 2 Air Rifles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V647000·2019-09-09

    Isuzu Recalls 2017-2019 Trucks for Potential Electrical Wiring Defect

    Isuzu is recalling 2017-2019 N-Series and Chevrolet Low Cab Forward trucks because a loose bolt in the relay box may cause electrical failure and vehicle stalling.

    Product
    CHEVROLET — CHEVROLET, ISUZU LOW CAB FORWARD 6500, LOW CAB FORWARD 4500, LOW CAB FORWARD 3500, N-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V648000·2019-09-09

    Mercedes-Benz Recalls 2020 GLE Models for Missing Head Restraint Manual Info

    Mercedes-Benz is recalling 2020 GLE 350 and GLE 450 vehicles because the owner's manuals lack instructions for adjusting third-row head restraints, violating federal safety standards.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E060000·2019-09-06

    TAP Recalls Pro Comp Lug Nuts Due to Incorrect Sizing

    TAP Worldwide is recalling 840 Pro Comp Extended Thread lug nuts that may be incorrectly sized. The defect could prevent proper tightening, leading to lug stud failure and increased crash risk.

    Product
    WHEELS:LUGS/NUTS/BOLTS/STUDS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V643000·2019-09-06

    GM Recalls 2020 Buick Enclave and Chevrolet Traverse for Frame Rail Crack

    General Motors is recalling 2020 Buick Enclave and Chevrolet Traverse vehicles because a crack in the right-hand frame rail may reduce crash performance and increase injury risk.

    Product
    BUICK — BUICK, CHEVROLET ENCLAVE, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V645000·2019-09-06

    GM Recalls Trucks and SUVs for Brake Vacuum Pump Defect

    General Motors is recalling 2014-2018 Chevrolet, GMC, and Cadillac vehicles because a vacuum pump defect may reduce brake assist, increasing stopping distance.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SUBURBAN, SILVERADO 1500, SIERRA 1500, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V644000·2019-09-06

    GM Recalls 2019 Chevrolet Express and GMC Savana for Seatbelt Warning Defect

    General Motors is recalling 2019 Chevrolet Express and GMC Savana vehicles because the seatbelt-unfastened warning light may fail to illuminate for five seconds after ignition.

    Product
    GMC — GMC, CHEVROLET SAVANA, EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V646000·2019-09-06

    Temsa Recalls Buses Due to Inadequate Emergency Exit Window Labels

    Temsa is recalling 2013-2020 TS35C, TS35E, and TS45 buses because emergency exit window labels may not clearly describe how to open them quickly.

    Product
    TEMSA — TEMSA TS35C, TS45, TS35E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V642000·2019-09-06

    GM Recalls 2018 Chevrolet Malibus Due to Engine Software Error

    General Motors is recalling 2018 Chevrolet Malibus with 1.5L turbo engines because a software error may disable fuel injectors, causing the engine to stall.

    Product
    CHEVROLET — CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19202·2019-09-05

    MOMO Quick Release Steering Wheel Adapters Recalled for Crash Hazard

    MW Company is recalling MOMO Quick Release Steering Wheel Adapters for race cars because the quick release mechanism can activate inadvertently, causing the steering wheel to detach and posing a crash hazard.

    Product
    MOMO Quick Release Steering Wheel Adapters for Race Cars
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19201·2019-09-05

    STIHL PolyCut Mowing Heads Recalled Due to Injury Hazard

    STIHL is recalling about 73,000 PolyCut mowing heads because loose bolts can cause the unit to come apart, posing an injury risk.

    Product
    STIHL PolyCut ™ Mowing Heads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19779·2019-09-05

    Walker Edison Recalls Children's Bunk Beds Due to Fall Hazards

    Walker Edison Furniture is recalling about 1,200 children's bunk beds because support boards can break, posing fall and injury hazards.

    Product
    Children's bunk beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2386-2019·2019-09-04

    Bard GlidePath Hemodialysis Catheter Recalled for Tip Damage

    Bard Peripheral Vascular Inc. is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393420, 14.5F, Straight, 42cm length, BARD, UDI: 00801741012228
    Category
    Medical Device
    Distribution
    53 states
  • SevereFDA (Devices)·Z-2378-2019·2019-09-04

    Bard Equistream XK Hemodialysis Catheter Recalled for Tip Damage

    Bard Peripheral Vascular Inc is recalling Equistream XK Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5913230, 16F, Straight, 23cm length, BARD, UDI: 00801741013843
    Category
    Medical Device
    Distribution
    53 states
  • SevereFDA (Drugs)·D-1845-2019·2019-09-04

    Pfizer Recalls Relpax Tablets Due to Microbial Contamination

    Pfizer is recalling specific lots of Relpax (eletriptan HBr) tablets because they may be contaminated with Burkholderia and Pseudomonas bacteria.

    Product
    RELPAX (eletriptan HBr) tablets, 40 mg, packaged in a) 6-count (1 card x 6 tablets) per carton, NDC 0049-2340-45; b) 12-count (2 cards x 6 tablets) per carton, NDC 0049-2340-05, Rx only, Made in Ireland, Distributed by Pfizer Roerig, Division of Pfizer Inc., NY, NY 10017.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2089-2019·2019-09-04

    Confectionery Arts International Recalls Jewel Dust Pearlescent Pigment

    Confectionery Arts International is recalling Jewel Dust pearlescent pigment because borosilicate glass material was found in an FDA sample.

    Product
    All colors and sizes of Confectionery Arts International, LLC brand Jewel Dust, a pearlescent pigment, manufactured and sold prior to 4/25/19; 4g packed in 1/4 oz. jars and 14g packed in 1 oz. jars.
    Category
    Food
    Distribution
    26 states